J.M. Trent

4.3k total citations
20 papers, 563 citations indexed

About

J.M. Trent is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, J.M. Trent has authored 20 papers receiving a total of 563 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Oncology. Recurrent topics in J.M. Trent's work include Cancer Genomics and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Molecular Biology Techniques and Applications (3 papers). J.M. Trent is often cited by papers focused on Cancer Genomics and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Molecular Biology Techniques and Applications (3 papers). J.M. Trent collaborates with scholars based in United States, Sweden and Australia. J.M. Trent's co-authors include John F. Harris, I. Balazs, S.C. Bock, Anne Kallioniemi, J Isola, Xin‐Yuan Guan, Joe W. Gray, David Kowbel, Mika Tirkkonen and Olli Kallioniemi and has published in prestigious journals such as Nature Genetics, JNCI Journal of the National Cancer Institute and The Journal of Urology.

In The Last Decade

J.M. Trent

19 papers receiving 552 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
J.M. Trent United States 11 282 173 168 104 76 20 563
Beth O. Van Emburgh United States 9 664 2.4× 132 0.8× 223 1.3× 165 1.6× 83 1.1× 10 922
Mihaela Velicescu United States 11 672 2.4× 193 1.1× 128 0.8× 132 1.3× 41 0.5× 12 898
C Kittas Greece 15 197 0.7× 67 0.4× 216 1.3× 61 0.6× 73 1.0× 37 523
Zamir Brelvi United States 8 298 1.1× 101 0.6× 121 0.7× 39 0.4× 34 0.4× 21 490
John C. Law United States 12 377 1.3× 86 0.5× 326 1.9× 141 1.4× 56 0.7× 16 658
Kristi L. Bennett United States 12 529 1.9× 71 0.4× 103 0.6× 156 1.5× 59 0.8× 13 674
Ajita Narayan United States 8 606 2.1× 146 0.8× 150 0.9× 126 1.2× 39 0.5× 9 754
Francis Wright United States 10 162 0.6× 58 0.3× 168 1.0× 110 1.1× 49 0.6× 21 437
Fred Elfman United States 14 328 1.2× 46 0.3× 141 0.8× 125 1.2× 57 0.8× 21 600
Zaletaev Dv Russia 12 435 1.5× 86 0.5× 154 0.9× 201 1.9× 79 1.0× 93 674

Countries citing papers authored by J.M. Trent

Since Specialization
Citations

This map shows the geographic impact of J.M. Trent's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by J.M. Trent with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.M. Trent more than expected).

Fields of papers citing papers by J.M. Trent

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J.M. Trent. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by J.M. Trent. The network helps show where J.M. Trent may publish in the future.

Co-authorship network of co-authors of J.M. Trent

This figure shows the co-authorship network connecting the top 25 collaborators of J.M. Trent. A scholar is included among the top collaborators of J.M. Trent based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with J.M. Trent. J.M. Trent is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Zhu, Gu, Grant W. Montgomery, Michael R. James, et al.. (2006). A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions. European Journal of Human Genetics. 15(1). 94–102. 51 indexed citations
2.
Ringnér, Markus, Carsten Peterson, Mårten Fernö, et al.. (2001). A layered perceptron approach to categorizing cDNA microarray measurements. Nature Genetics. 27(S4). 83–83. 1 indexed citations
3.
Bergþorsson, Jón Þór, Guðrún Jóhannesdóttir, Aðalgeir Arason, et al.. (2000). Analysis of HPC1, HPCX, and PCaP in Icelandic hereditary prostate cancer. Human Genetics. 107(4). 372–375. 26 indexed citations
4.
Kauraniemi, Päivikki, Ingrid Hedenfalk, Karin Persson, et al.. (2000). MYB oncogene amplification in hereditary BRCA1 breast cancer.. PubMed. 60(19). 5323–8. 79 indexed citations
5.
Cheng, Richard Z., Xiaoping Guan, George Lau, et al.. (1998). Chromosome 1p terminal deletion and loss of chromosome 17p and 16p are common findings in nasal NK/T cell lymphoma by comparative genomic hybridization. Laboratory Investigation. 78(1). 126. 3 indexed citations
6.
Grönberg, Henrik, Sarah D. Isaacs, Jeffrey R. Smith, et al.. (1998). Characteristics of Prostate Cancer in Families Potentially Linked to the Hereditary Prostate Cancer 1 (HPC1) Locus. The Journal of Urology. 159(4). 1399–1400. 10 indexed citations
7.
Grönberg, Henrik, Jianfeng Xu, Jeffrey R. Smith, et al.. (1998). Early Age at Diagnosis in Families Providing Evidence of Linkage to the Hereditary Prostate Cancer Locus (HPC1) on Chromosome 1. The Journal of Urology. 160(1). 265–266. 24 indexed citations
8.
Tanner, Minna M., Mika Tirkkonen, Anne Kallioniemi, et al.. (1996). Independent amplification and frequent co-amplification of three nonsyntenic regions on the long arm of chromosome 20 in human breast cancer.. PubMed. 56(15). 3441–5. 162 indexed citations
9.
Cummings, Leda M., J.M. Trent, & Douglas A. Marchuk. (1996). Identification and mapping of type 1 neurofibromatosis (NF1) homologous loci. Cytogenetic and Genome Research. 73(4). 334–340. 16 indexed citations
10.
Su, Yan, et al.. (1996). Reversion of monochromosome-mediated suppression of tumorigenicity in malignant melanoma by retroviral transduction.. PubMed. 56(14). 3186–91. 16 indexed citations
11.
Guan, Xin‐Yuan, Jia Xu, Sarah L. Anzick, J.M. Trent, & Paul S. Meltzer. (1995). Direct isolation of amplified cDNAs from 20q in breast cancer by chromosome microdissection. Cancer Genetics and Cytogenetics. 84(2). 137–137. 1 indexed citations
12.
Zimonjic, Drazen B., et al.. (1995). Mapping of the immune interferon gamma gene (IFNG) to chromosome band 12q14 by fluorescence in situ hybridization. Cytogenetic and Genome Research. 71(3). 247–248. 18 indexed citations
13.
Pappas, George J., Elizabeth Thompson, Ann C. Burgess, Alex D. Greenwood, & J.M. Trent. (1995). Generation and molecular cytogenetic characterization of a radiation-reduction hybrid panel for human chromosome 6. Cytogenetic and Genome Research. 69(3-4). 201–206. 1 indexed citations
14.
Taetle, Raymond, J.M. Trent, Ruth Weinstein, et al.. (1995). Clinical correlations of chromosome abnormalities in human breast, melanoma and ovarian cancer: preliminary analyses of 580 patients. Cancer Genetics and Cytogenetics. 84(2). 135–135. 3 indexed citations
15.
Lagoda, Pierre, J.M. Trent, & Eckart Meese. (1994). Chromosome specific c-DNA libraries: reduction of unspecific priming events by purification of heteronuclear RNA. Molecular Biology Reports. 19(2). 89–92. 1 indexed citations
16.
Yu, Hua, et al.. (1993). Human PCK1 Encoding Phosphoenolpyruvate Carboxykinase Is Located on Chromosome 20q13.2. Genomics. 15(1). 219–221. 15 indexed citations
17.
18.
Trent, J.M., et al.. (1991). Cytogenetic and molecular analysis of human malignant melanoma: The search for a suppressor gene on chromosome 6.. Cancer Genetics and Cytogenetics. 52(2). 255–255. 1 indexed citations
19.
Zwelling, Leonard A., Marilyn L. Slovak, J. H. Doroshow, et al.. (1990). HT1080/DR4: A P-Glycoprotein-Negative Human Fibrosarcoma Cell Line Exhibiting Resistance to Topoisomerase II-Reactive Drugs Despite the Presence of a Drug-Sensitive Topoisomerase II. JNCI Journal of the National Cancer Institute. 82(19). 1553–1561. 48 indexed citations
20.
Bock, S.C., John F. Harris, I. Balazs, & J.M. Trent. (1985). Assignment of the human antithrombin III structural gene to chromosome 1q23–25. Cytogenetic and Genome Research. 39(1). 67–69. 87 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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